Cas 334473-86-8,(-)-methyl (1R,2R,1'R,3'R)-1-N-benzyloxycarbonylamino-2-[2',2'-dimethyl-3'-(2-methyl-1,3-dioxolan-2-yl)cyclobutyl]cyclopropanecarboxylate

334473-86-8

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Basic information

Product Name: (-)-methyl (1R,2R,1'R,3'R)-1-N-benzyloxycarbonylamino-2-[2',2'-dimethyl-3'-(2-methyl-1,3-dioxolan-2-yl)cyclobutyl]cyclopropanecarboxylate
Synonyms:
CAS NO:334473-86-8
Molecular Formula:
Molecular Weight: 417.502
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (-)-methyl (1R,2R,1'R,3'R)-1-N-benzyloxycarbonylamino-2-[2',2'-dimethyl-3'-(2-methyl-1,3-dioxolan-2-yl)cyclobutyl]cyclopropanecarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (-)-methyl (1R,2R,1'R,3'R)-1-N-benzyloxycarbonylamino-2-[2',2'-dimethyl-3'-(2-methyl-1,3-dioxolan-2-yl)cyclobutyl]cyclopropanecarboxylate(334473-86-8)
EPA Substance Registry System: (-)-methyl (1R,2R,1'R,3'R)-1-N-benzyloxycarbonylamino-2-[2',2'-dimethyl-3'-(2-methyl-1,3-dioxolan-2-yl)cyclobutyl]cyclopropanecarboxylate(334473-86-8)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 334473-86-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 334473-86-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,4,4,7 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 334473-86:
(8*3)+(7*3)+(6*4)+(5*4)+(4*7)+(3*3)+(2*8)+(1*6)=148
148 % 10 = 8
So 334473-86-8 is a valid CAS Registry Number.

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334473-86-8Relevant academic research and scientific papers

Stereoselective synthesis of cyclobutyl α-aminocyclopropyl carboxylic acid derivatives

Moglioni,Garcia-Exposito,Alvarez-Larena,Branchadell,Moltrasio,Ortuo

, p. 4903 - 4914 (2007/10/03)

The highly stereoselective cyclopropanation of chiral cyclobutyl dehydro amino acids, synthesized from (-)-α-pinene or (-)-verbenone, has been achieved by means of a 1,3-dipolar cycloaddition with diazomethane. The proximity of the double bond to the neig

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